Startseite Influence of added and differently attached methyl groups on the crystal structure of 2,6-diphenyl substituted p-nitrophenol
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Influence of added and differently attached methyl groups on the crystal structure of 2,6-diphenyl substituted p-nitrophenol

  • Sanrda Kurjatschij , Diana Eißmann , Wilhelm Seichter und Edwin Weber
Veröffentlicht/Copyright: 24. November 2010
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Abstract

In order to find out the consequences of a methyl substitution on the crystalline packing behaviour of the parent compound 2,6-diphenyl-4-nitrophenol, three analogous nitrophenols being substituted at different positions of the lateral phenyl rings were comparatively studied with regard to their crystal structures. While the molecular structures do not suggest marked differences, the network structures do, showing dependency on the presence and positional substitution of the methyl groups. This is revealed by the formation of weakly O—H…π bonded dimers or supramolecular chains, more strongly hold together through interacting OH and nitro groups.


* Correspondence address: TU Bergakademie Freiberg, Institut für Organische Chemie, Leipziger Str. 29, 09596 Freiberg, Deutschland,

Published Online: 2010-11-24
Published in Print: 2011-03

© by Oldenbourg Wissenschaftsverlag, Freiberg, Germany

Heruntergeladen am 22.9.2025 von https://www.degruyterbrill.com/document/doi/10.1524/zkri.2011.1287/html
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